{"orpha":251535,"name":"Maternal disease-related embryofetopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-251535/","orphanet_url":"https://www.orpha.net/en/disease/detail/251535","names":{"fr":{"name":"Embryofoetopathie par maladie maternelle"},"de":{"name":"Embryopathie, mit maternaler Krankheit assoziierte"},"es":{"name":"Embriofetopatía por enfermedad materna"},"it":{"name":"Embriofetopatia da malattia materna"},"nl":{"name":"Maternale ziekte-gerelateerde embryofoetopathie"},"pt":{"name":"Embriofetopatia relacionada com doença materna"},"pl":{"name":"Embriofetopatia związana z chorobą matczyną"},"cs":{"name":"Embryofetopatie na podkladě onemocnění matky"},"uk":{"name":"Ембріофетопатія, повязана із захворюванням матері"},"zh":{"name":"母源疾病相关胚胎胎儿病"},"tr":{"name":"Maternal hastalık-ilişkili embriyofetopati"}},"xrefs":[{"source":"MONDO","code":"16678","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680708","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":52662,"name":"Rare teratologic disease","classifications":[147,216]}],"children":[{"orpha":1926,"name":"Diabetic embryopathy","type":"Malformation syndrome"},{"orpha":723156,"name":"Fetal acetylcholine receptor antibody-related disorder","type":"Disease"},{"orpha":2216,"name":"Maternal hyperthermia-induced birth defects","type":"Malformation syndrome"},{"orpha":2209,"name":"Maternal phenylketonuria syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}